All terms in OMIM

Label Id Description
lipodystrophy, partial, acquired, susceptibility to 608709
BOC 608708
CDON 608707
DNAAF4 608706
omphalocele, X-linked 310980
CTSB 116810
PTPRT 608712
CTDSP2 608711
granulomatosis with polyangiitis 608710
SLURP1 606119
RPP40 606117
HPS3 606118
congenital disorder of glycosylation, type iie 608779
CTNNA1 116805
CTNNB1 116806
MPV17L 618100
SIMC1 618102
MMP27 618101
MMEL1 618104
intellectual developmental disorder, autosomal recessive 64 618103